Hoffmann Bromamide Reaction

1. What Is Hoffmann Bromamide Reaction in Chemistry?

Hoffmann Bromamide Reaction is a chemical reaction that is used to perform primary amine.

2. What is Other Name of Hoffmann Bromamide Reaction

Hoffmann Bromamide Reaction is also called Hoffmann Degradation.

3. What is Intermediate Compound in Hoffmann Bromamide Reaction?

Intermediate compound in the Hoffmann Bromamide Reaction is the Bromamide Anion (RCONBr⁻).

4. What are Reagents in the Hoffmann Bromamide Reaction?

Hoffmann Bromamide Reaction uses specific reagents for the process. These reagents are a primary amide (RCONH2), Bromine (Br2), a strong base (usually sodium hydroxide, NaOH), and water (H2O).

5. What is an Example of a Hofmann Reaction?

Some example of Hoffamm Reaction are,

CH3CONHPh + 3Br2 + 6NaOH → C6H5NH2 + CH3COONa + 3NaBr + 3H2O

6. What is the Name Reaction of Amide to Amine?

Name Reaction of Amide to Amine is Hofmann’s Bromamide Reaction.

7. What Is Mechanism Of Hoffmann Bromamide Reaction?

Mechanism of Hoffmann Bromamide reactions includes the following steps,

  1. Hydroxide Ion Attack on Amide
  2. Anion Attack on Bromine
  3. Base Attack on N-Bromamide
  4. Rearrangement of Bromamide Anion
  5. Addition of Water to Isocyanate
  6. Loss of Carbon Dioxide


Hoffmann Bromamide Reaction

Hoffmann Bromamide Reaction is named after the famous chemist August Wilhelm Von Hoffmann. If an amide is treated with Bromine in an aqueous or ethanolic solution of sodium hydroxide, the formation of amine takes place. It is used to synthesize primary aromatic and aliphatic amines.

In this article, we will explore the Hoffmann Bromamide Reaction, its mechanism, its applications, examples, and limitations in detail.

Table of Content

  • What is Hoffmann Bromamide Reaction?
  • Hoffmann Bromamide Reaction Mechanism
  • Examples of Hoffmann Bromamide Reaction
  • Hoffmann Bromamide Reaction Applications
  • Limitations of Hoffmann Bromamide Reaction

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What is Hoffmann Bromamide Reaction?

Hoffmann Bromamide Reaction involves the strategic use of alkali as a strong base to attack an amide. This attack triggers deprotonation and the generation of an anion. The reaction unfolds by heating a primary amide with a halogen, a strong base, and water. The primary amine that results is entirely free from contamination. No secondary or tertiary amines are present in the Hoffmann Bromamide Reaction. This is a significant characteristic of the reaction. Hoffman Bromamide Reaction is also called Hoffman Bromamide Degradation Reaction....

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